EP2396598A1 - Method of treating an exhaust gas stream - Google Patents
Method of treating an exhaust gas streamInfo
- Publication number
- EP2396598A1 EP2396598A1 EP10704402A EP10704402A EP2396598A1 EP 2396598 A1 EP2396598 A1 EP 2396598A1 EP 10704402 A EP10704402 A EP 10704402A EP 10704402 A EP10704402 A EP 10704402A EP 2396598 A1 EP2396598 A1 EP 2396598A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cooling
- gases
- liquid
- abated
- region
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 44
- 239000007789 gas Substances 0.000 claims abstract description 108
- 238000001816 cooling Methods 0.000 claims abstract description 57
- 238000005086 pumping Methods 0.000 claims abstract description 43
- 239000007788 liquid Substances 0.000 claims abstract description 39
- 239000002826 coolant Substances 0.000 claims abstract description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 44
- 229910001868 water Inorganic materials 0.000 claims description 44
- 238000001914 filtration Methods 0.000 claims description 19
- 238000002347 injection Methods 0.000 claims description 10
- 239000007924 injection Substances 0.000 claims description 10
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 5
- 239000007921 spray Substances 0.000 claims description 5
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 4
- 239000001569 carbon dioxide Substances 0.000 claims description 4
- 238000011144 upstream manufacturing Methods 0.000 claims description 4
- 239000003595 mist Substances 0.000 claims description 3
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims 1
- 239000000567 combustion gas Substances 0.000 description 30
- 238000001704 evaporation Methods 0.000 description 8
- 230000008020 evaporation Effects 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000005200 wet scrubbing Methods 0.000 description 5
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 239000000470 constituent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000010899 nucleation Methods 0.000 description 3
- 230000006911 nucleation Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000000889 atomisation Methods 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000012809 cooling fluid Substances 0.000 description 2
- 239000000112 cooling gas Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000002737 fuel gas Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000001473 noxious effect Effects 0.000 description 2
- 210000002381 plasma Anatomy 0.000 description 2
- 238000005201 scrubbing Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 235000012431 wafers Nutrition 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical compound [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 description 1
- 229910000413 arsenic oxide Inorganic materials 0.000 description 1
- 229960002594 arsenic trioxide Drugs 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000005137 deposition process Methods 0.000 description 1
- KTTMEOWBIWLMSE-UHFFFAOYSA-N diarsenic trioxide Chemical compound O1[As](O2)O[As]3O[As]1O[As]2O3 KTTMEOWBIWLMSE-UHFFFAOYSA-N 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G7/00—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
- F23G7/06—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G7/00—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
- F23G7/06—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases
- F23G7/061—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases with supplementary heating
- F23G7/065—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases with supplementary heating using gaseous or liquid fuel
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/77—Liquid phase processes
- B01D53/79—Injecting reactants
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J15/00—Arrangements of devices for treating smoke or fumes
- F23J15/06—Arrangements of devices for treating smoke or fumes of coolers
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2204/00—Supplementary heating arrangements
- F23G2204/10—Supplementary heating arrangements using auxiliary fuel
- F23G2204/103—Supplementary heating arrangements using auxiliary fuel gaseous or liquid fuel
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2207/00—Control
- F23G2207/50—Cooling fluid supply
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2209/00—Specific waste
- F23G2209/14—Gaseous waste or fumes
- F23G2209/142—Halogen gases, e.g. silane
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J2219/00—Treatment devices
- F23J2219/80—Quenching
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E20/00—Combustion technologies with mitigation potential
- Y02E20/30—Technologies for a more efficient combustion or heat usage
Definitions
- the present invention relates to a method of treating an exhaust gas stream.
- the exhaust gases may be treated in any of a number of different ways. Typically, exhaust gases are reacted in a burner (or other treatment device which imparts energy to the gas stream including; plasmas, electrically heated catalytic columns, electric furnaces, etc) to thermally decompose, or otherwise treat, noxious substances in the exhaust stream prior to disposal.
- a burner or other treatment device which imparts energy to the gas stream including; plasmas, electrically heated catalytic columns, electric furnaces, etc
- An example of a burner / combustor is used specifically herein, however the abatement device could be a range of techniques which introduce energy to a gas stream.
- the exhaust gases become hot and therefore require to be cooled prior to emission to the environment. Methods available for cooling involve either direct contact with the cooling fluid (mixing with water, air, etc) or indirect contact with a cooling fluid (heat exchanger, radiator, etc).
- a method commonly employed has a water column or weir arrangement which may be adopted downstream of the combustor for cooling the gases.
- the gases are cooled by close proximity to or contact with running water, and particulates or powder in the combustion gases are entrained in the water. Cooling the combustion gases in this way requires a considerable quantity of water which adds significantly to the cost of treatment.
- the arrangement requires the management and disposal of wet powder and the presence of particulates in the water system may reduce reliability; additionally particulates may be toxic, as in the case of arsenic oxide. In the case of toxic solids exhaust gas stream filtration delivers a lower volume of contaminated material than conventional wet scrubbing.
- combustion gases are cooled by an air-stream which is introduced to cool the combustion gases. If the combustion gases contain particulates, the air-stream and the combustion gases are passed through a filtration system to remove the particulates and allow the air to be re-circulated or released to atmosphere.
- the filtration systems which are used in the filtration of finely divided silica, can typically operate to remove particulates from gas streams only if the gas streams are relatively cool and constituents in the gas stream do not condense in the system. Therefore increased quantities of air must be used to cool the combustion gases to allow filtration to take place. If the exhaust gases from a processing chamber generate a high heat load in the burner (for instance where the exhaust gases contain hydrogen or silane), still further quantities of air must be used to cool the combustion gases sufficiently for filtration to occur.
- a vacuum pumping arrangement is placed downstream of the treatment device.
- the vacuum pumping arrangement must have sufficient capacity to draw not only the combustion gases but also the air introduced to cool the gases.
- the cost of a vacuum pumping arrangement increases as the pumping capacity increases. The problem is further exacerbated if further quantities of air are required to cool exhaust gases containing such constituents as hydrogen or silane.
- Semi-conductor wafer or other processing techniques occur within a processing chamber, this operation usually taking place at low pressure in the region of 1 mTorr to 1 Torr (however processes such as SACVD may occur close to atmospheric pressure). Such low pressures are achieved with a vacuum pumping arrangement. If the exhaust gases are flammable, then it is desirable to treat the flammable constituents prior to the vacuum pumping arrangement (or between vacuum pumping stages). The flammability of gases depends on a self sustaining chain of single reactions; for energy to transfer successfully from one set of molecules (combustion products) to another set of molecules (reactants) the two molecule sets require to be close for energy absorption.
- Dilution acts both to surround and separate the reactive molecules; this causes energy to be absorbed by inert molecules (the walls of the vessel containing the reaction can be considered as inert molecules). Eventually a self-sustaining reaction is no longer possible and this is defined as the Lower Flammability Limit.
- Reducing the pressure of a system increases separation of molecules within a reaction vessel.
- the inert and reactive molecules of the process remain in constant proportion; however the walls of the vessel retain a constant surface area.
- This constant surface area at reduced pressure results in a higher proportion of the energy being absorbed by the walls of a vessel before the energy can activate reactive molecules. Consequently the concentration of reactive molecules necessary for sustaining a chain reaction at low pressure is higher than the concentration required at atmospheric pressure.
- gas streams which are non-flammable at low pressure become flammable if the pressure is increased to atmospheric pressure. Therefore flammable gases can be reacted at low pressure in a controlled way, before they become potentially hazardous / flammable at atmospheric pressure.
- vacuum pumping arrangements in common with many mechanical items
- This problem is exacerbated in later stages of a vacuum pumping arrangement where the gases are close to atmospheric pressure.
- the problem can be mitigated by introducing large quantities of a purge gas, such as nitrogen, upstream of the vacuum pumping arrangement.
- a purge gas such as nitrogen
- An alternative solution involves burning the exhaust gases in a burner and then conveying the combustion gases through the vacuum pumping arrangement. Although this latter solution removes flammable substances from the exhaust gases, the combustion gases are hot and heat the vacuum pumping arrangement.
- vacuum pumping arrangement must therefore be cooled or the gas flow into the pump must be cooled so as to avoid damaging the pump.
- vacuum pumps are designed to provide a vacuum at a given process flow therefore significantly increasing the process flow degrades vacuum performance and increases the power consumption. Therefore, a partial solution which simply involves adding large flows of cooling gas is not advisable.
- the present invention provides a method of treating an exhaust gas stream from a processing chamber, the method comprising the steps of: conveying the exhaust gas from the processing chamber using a vacuum pumping arrangement or atmospheric line; abating the exhaust gas in an abatement region of an abatement device; and injecting a cooling agent downstream of the abatement region to cool the abated gases in a cooling region by phase change of the cooling agent.
- Figure 1 shows schematically a system for treating exhaust gases from a processing chamber
- Figure 2 shows schematically another system for treating exhaust gases from a processing chamber.
- Embodiments of the present invention provide a method for cooling gases after treatment, or abatement, which involves the injection of a cooling agent into a cooling region downstream of an abatement region.
- the cooling agent may be a liquid such as water, injected optionally as a finely divided mist or spray into the heated plume emanating from a treatment device.
- the liquid absorbs heat by evaporative cooling when the liquid changes phase from liquid to gas. Since the principle method by which heat is absorbed is by phase change, the present invention also includes injection of substances in other states such that they may change phase to absorb heat in the system. For example, carbon dioxide may be injected as a solid and undergoes sublimation changing phase to a gas. Alternatively, ice particles could be injected changing phase to liquid water and then also possibly changing phase to a gas. However, the description of the embodiments herein is directed specifically to the injection of liquid as a cooling agent into the gas stream.
- Absorbing energy by phase change is advantageous because it does not significantly add to the volume of the gas stream handled by a downstream apparatus such as a filtration apparatus or vacuum pumping arrangement. Accordingly, the capacity of the downstream apparatus need not generally be increased to manage increased gas flow volume.
- the methods allow cooling of exhaust gases at sub-atmospheric, atmospheric (dry filtration), atmospheric (wet scrubbing) pressures for example to below a lower flammability limit.
- the gases passing into a vacuum pumping arrangement can range in temperature from 25 - 250 0 C.
- the heat energy present in the gases emanating from the treatment device is determined and the injection of liquid is controlled so that once evaporated does not subsequently condense due to the pressure generated by the vacuum pumping arrangement and so that the combustion gases are not hot enough to damage the pumping mechanism.
- the injection of liquid is controlled so that the cooled gas mixture is non-condensing and of a reasonably low temperature (e.g. ⁇ 70 0 C depending on the filtration unit) so as not to damage the membrane of the filter.
- a reasonably low temperature e.g. ⁇ 70 0 C depending on the filtration unit
- the injection of liquid aids the wet scrubbing mechanism by both reducing the gas flow into the wet scrubber and preconditioning the waste products in the gas stream to improve wet scrubbing.
- the wet scrubber can form part of the treatment system or can be remote therefrom. In the latter case a single wet scrubber receives gas from one or more abatement units.
- the preconditioning of the waste gas involves evaporating a liquid such as water into the gas plume.
- the wet scrubber rapidly cools the gas mixture resulting in the gas plume becoming saturated.
- the evaporated liquid has a propensity to condense around solid particles within the system which act as nucleation sites thereby forming droplets of liquid with a solid core.
- the condensation / nucleation process improves removal of particulates by the wet scrubber, as the particulates are contained in a liquid droplet which makes it significantly larger and more readily mixed with the wet scrubbing medium.
- the temperature of the gases passing into the scrubber depends on the temperature tolerance of the wet scrubber unit, for example a system in which the vessel wall is formed by a water weir can be operable with a gas stream in excess of 100 0 C, whereas a wet scrubber made of polypropylene require a temperature of less than about 100 0 C.
- a processing chamber 10 is shown from which processing gas is exhausted during or after processing.
- the system normally comprises a primary vacuum pumping arrangement 11 for exhausting gas and conveying it through the system.
- the vacuum pumping arrangement 11 also isolates combustion or other abated gases from the processing chamber 10.
- the processing chamber may be connected directly to an abatement unit.
- the process gases may be conveyed by connecting the process chamber to atmosphere with an atmospheric line and suitable valve arrangement.
- the exhaust gases 12 are conveyed to an abatement unit, such as a burner 14.
- the burner 14 may be a radiant burner as shown (or other abatement devices which impart energy to the gas stream including; plasmas, electrically heated catalytic columns, electric furnaces).
- a system for treating exhaust gas is shown in GB0724717.4, the contents of which are hereby incorporated by reference.
- a fuel gas 16 is introduced to the burner and ignited for combusting the exhaust gases in an abatement, or combustion, region 18 of the burner.
- hot combustion gases (abatement gases) 20 are produced which may be at a temperature in the region of 500 - 2000 0 C.
- combustion gases which are at low, or sub-atmospheric, pressure
- a cooling agent which may be a liquid such as water 26 is introduced by injection into the cooling region 24 for cooling the combustion gases by phase change of the cooling agent.
- the water may be introduced as a fine spray thereby providing a relatively large surface area to volume ratio so that the liquid evaporates more easily. Fine sprays can be generated using spray nozzles, and are available from a range of companies for example AutoJet Technologies, a division of Spraying Systems Co.
- the vacuum pumping arrangement 22 is operable with the primary vacuum pumping arrangement 11 to evacuate processing gases from the processing chamber 10 and exhaust cooled combustion gases either for further treatment or release to atmosphere.
- the vacuum generated by vacuum pumping arrangements 11, 22 draws gases from the processing chamber and through the abatement device (shown as a combustor in the illustration).
- the vacuum pumping arrangement typically comprises metal parts which move one relative to another. If the parts become worn or accumulate deposits, it may cause the parts to come into contact generating a spark.
- the burner 14 has combusted flammable substances in the gas stream upstream of the vacuum pumping arrangement and therefore, any spark generated cannot ignite the gas stream and does not damage the vacuum pumping arrangement or other equipment.
- the vacuum pumping is not heated excessively and does not require additional cooling.
- Cooling may occur by both the latent heat of evaporation of the liquid and also through the process of heating the injected liquid.
- Carbon dioxide has useful properties, including reducing flammability and could be used as a solid (dual phase change) or liquid.
- liquid water is not allowed to enter or condense within higher pressure regions of the vacuum pumping arrangement, thereby avoiding hydraulic lock, potential corrosion of metal and other parts in the vacuum pumping arrangement. Accordingly, the amount of water introduced to the cooling region 24 is controlled such that substantially all of it is evaporated prior to entry into the vacuum pumping arrangement.
- the amount of water 26 required can be predetermined for the expected flow rate of combustion gases 20 or a plurality of expected flow rates, and the introduction of water to the cooling region 24 controlled accordingly.
- one or more sensors 28 can be provided, for example at the exhaust of the cooling region as shown, for sensing the temperature or another characteristic of the combustion gases 20. The sensors are adapted to output a signal to a control unit 29 for controlling flow of water 26 into the cooling region.
- pre-determined flows of water could be injected; otherwise a feedback loop could be used that regulated the amount of water injected so as to maintain a pre-determined exhaust gas temperature (e.g. 70 0 C).
- a pre-determined exhaust gas temperature e.g. 70 0 C
- the water can be introduced to the cooling region 24 by different arrangements.
- the water may be atomised and introduced as a mist (fine mists aid evaporation). Atomisation can be controlled to regulate the size and quantity of water particles entering the cooling region 24.
- water may be introduced at pressure as one or more fine jets through a nozzle.
- the water may be introduced along a capillary such that pressure in the cooling region, and the diameter and length of the capillary controls the amount of water entering the cooling region.
- a system 30 is shown for treating exhaust gases.
- a processing chamber and vacuum pumping arrangement is shown as one unit 32 in Figure 2 from which process gas 34 is exhausted.
- the exhaust gases are abated by an abatement unit, or as shown are combusted in a burner 36, which may be a radial burner.
- a fuel gas 38 is introduced to the burner and ignited for combusting the exhaust gases in a combustion, or abatement, region 40 of the burner.
- a filtration apparatus 42 for example a powder filtration device, filters particulates, powder or other solid matter from combustion gases producing filtered gas 44 and powder 46.
- a wet scrubber 56 is provided for scrubbing the abatement gases.
- a scrubbing medium 58 such as water, is introduced for entraining particulates in the abatement gases. Air 60 and wet powder 62 are exhausted from the wet scrubber 56.
- Combustion gases 48 exhausted from the burner 36 are cooled in cooling region 50 by introduction of an air-stream 52.
- a cooling agent such as water or other liquid 54 is introduced by injection into the cooling region 50 for cooling the hot combustion gases by phase change of the cooling agent. Cooling occurs principally by latent heat of evaporation of the liquid, although it will be appreciated that some cooling occurs by heating the cooling agent without phase change.
- a typical filtration apparatus 42 has an upper working temperature of about 70 0 C.
- a high heat load may be generated in the burner 36, such as when combusting hydrogen from a semiconductor or solar cell deposition process. In this regard, several hundred litres per minute of hydrogen can raise the combustion gas temperature to above 130 0 C.
- the additional heat load requires significantly increased amounts of air to be introduced to the cooling region for cooling which, in turn, requires much larger (and more expensive) powder filtration to be employed.
- the hot combustion gases are cooled sufficiently by the water 54 so that additional amounts of air are not required and so that the filtration apparatus operates below its upper working temperature.
- the temperature and mass or volume flow rate of the combustion gases 48 are also known it can be determined the amount of water 54 which must be introduced to the cooling region 50 to achieve adequate temperature reduction of the combustion gases. Accurate control of the amount of liquid (such as water) introduced also avoids wasting water and adding to the cost of ownership.
- the amount of water introduced to the cooling region 50 is controlled such that substantially all of it is evaporated prior to entry into the filter. It is essential that there is sufficient allowance made for cooling between the combustor and the filters, so that the water within the gas plume does not start to condense out. This requires the humidity in the cooled exhaust flow to be less than 100% relative humidity at the point of cooling.
- the injection of liquid 52 into the cooling region potentiates the efficiency of the wet scrubber by providing nucleation and condensation processes in the abated gases upstream of the wet scrubber.
- the amount of liquid injected into the cooling region is controlled as previously described herein to limit heating of the wet scrubber to within tolerances.
- the water 54 may be introduced to the cooling region 50 by spraying, atomisation or other techniques as described above with reference to Figure 1.
Landscapes
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treating Waste Gases (AREA)
- Chimneys And Flues (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0902234.4A GB0902234D0 (en) | 2009-02-11 | 2009-02-11 | Method of treating an exhaust gas stream |
PCT/GB2010/050087 WO2010092365A1 (en) | 2009-02-11 | 2010-01-21 | Method of treating an exhaust gas stream |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2396598A1 true EP2396598A1 (en) | 2011-12-21 |
EP2396598B1 EP2396598B1 (en) | 2018-03-28 |
Family
ID=40527170
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP10704402.6A Active EP2396598B1 (en) | 2009-02-11 | 2010-01-21 | Method of treating an exhaust gas stream |
Country Status (8)
Country | Link |
---|---|
US (1) | US9631810B2 (en) |
EP (1) | EP2396598B1 (en) |
JP (1) | JP5654494B2 (en) |
KR (1) | KR101285041B1 (en) |
CN (1) | CN102317686B (en) |
GB (1) | GB0902234D0 (en) |
TW (1) | TWI492782B (en) |
WO (1) | WO2010092365A1 (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102012102251B4 (en) * | 2012-03-16 | 2013-11-07 | Das Environmental Expert Gmbh | Process and device for the treatment of noxious gases |
US9411341B2 (en) * | 2012-05-24 | 2016-08-09 | Globalfoundries Singapore Pte. Ltd. | Vacuum pump controller |
TWI496306B (en) * | 2012-05-24 | 2015-08-11 | Sunshine Pv Corp | Annealing device for a thin-film solar cell and cold trap thereof |
JP6153754B2 (en) * | 2013-03-28 | 2017-06-28 | 株式会社荏原製作所 | Vacuum pump with abatement function |
JP6151945B2 (en) | 2013-03-28 | 2017-06-21 | 株式会社荏原製作所 | Vacuum pump with abatement function |
GB2513300B (en) * | 2013-04-04 | 2017-10-11 | Edwards Ltd | Vacuum pumping and abatement system |
JP6368458B2 (en) * | 2013-05-24 | 2018-08-01 | 株式会社荏原製作所 | Vacuum pump with abatement function |
JP6166102B2 (en) * | 2013-05-30 | 2017-07-19 | 株式会社荏原製作所 | Vacuum pump with abatement function |
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TW201032889A (en) | 2010-09-16 |
JP5654494B2 (en) | 2015-01-14 |
JP2012517581A (en) | 2012-08-02 |
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